amyotrophic lateral sclerosis type 5

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (0)

DOID:0060197 - amyotrophic lateral sclerosis type 5

Disease Ontology Definition:An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21.

Synonyms: ALS5, amyotrophic lateral sclerosis 5

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: spg11

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011196 - amyotrophic lateral sclerosis type 5

MONDO:0011196 - amyotrophic lateral sclerosis type 5

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): amyotrophic lateral sclerosis (is_a)